Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs2030323 0.925 0.080 11 27706992 intron variant A/C snv 0.83 3
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 2
rs11030104 0.790 0.240 11 27662970 intron variant A/G snv 0.16 2